JOSEPH NASAL/TENDON KNIFE 1271-152C

GUDID 00192896057173

JOSEPH NASAL/TENDON KNIFE CURVED EDGE

SONTEC INSTRUMENTS, INC.

Orthopaedic osteotome blade, reusable

• Primary Device ID: 00192896057173
• NIH Device Record Key: c5759f03-49f8-4472-8c59-217dfd189b58
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: JOSEPH NASAL/TENDON KNIFE
• Version Model Number: 1271-152C
• Catalog Number: 1271-152C
• Company DUNS: 040729840
• Company Name: SONTEC INSTRUMENTS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does n
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Length: 6 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896057173 [Primary]

FDA Product Code

• HTS: KNIFE, ORTHOPEDIC

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00192896057173]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-10-29
• Device Publish Date: 2018-09-27

On-Brand Devices [JOSEPH NASAL/TENDON KNIFE]

• 00192896084049: JOSEPH NASAL/TENDON KNIFE ROUND TIP
• 00192896057173: JOSEPH NASAL/TENDON KNIFE CURVED EDGE
• 00192896057166: JOSEPH NASAL/TENDON KNIFE BLUNT EDGE